Jade Biosciences
Director, Medical Affairs – Jade Biosciences – Remote
Company Overview Jade Biosciences is focused on developing innovative, best‑in‑class therapies to address critical unmet needs in autoimmune diseases. The lead candidate, JADE101, inhibits the cytokine APRIL and is being developed for the treatment of immunoglobulin A nephropathy (IgAN). JADE101 aims to reduce harmful IgA antibodies, lower proteinuria, and preserve long‑term kidney function. A Phase 1 healthy‑volunteer study is ongoing, with interim biomarker data expected in the first half of 2026. The pipeline also includes JADE201 and an undisclosed antibody discovery program, JADE‑003, both in preclinical development.
Role Overview We are looking for a proactive and scientifically driven Director, Medical Affairs to support Jade’s clinical development programs and help establish the medical affairs function. The new position will serve as a bridge between clinical development and future commercial readiness, ensuring scientific rigor, regulatory alignment, and strategic foresight. The role reports to the Executive Medical Director, Clinical Development and is fully remote with occasional travel.
Key Responsibilities
Collaborate with internal stakeholders to develop and communicate medical plans for the therapeutic area and track progress for reporting.
Incorporate insights from scientific trends and the treatment landscape through participation in external events and activities.
Lead the development and dissemination of scientific and medical data via publications, presentations, and educational programs for healthcare professionals and other stakeholders.
Build and maintain strong relationships with KOLs, researchers, and patient advocacy groups to gather insights and inform strategy.
Manage conference calendar and coordinate onsite meetings, advisory boards, symposia, and medical education events.
Collaborate with the regulatory team to ensure all medical communications and activities comply with relevant regulations (e.g., FDA, ICH‑GCP).
Oversee or contribute to the design and implementation of studies generating real‑world evidence (RWE), health economics and outcomes research (HEOR), and other data to support product value proposition and market access efforts.
Act as a scientific consultant and collaborator across internal teams (R&D, Clinical Development, Regulatory Affairs, Commercial) to align strategies and support product development and commercialization.
Provide accurate and up‑to‑date medical information to address inquiries from healthcare professionals and external stakeholders.
Review promotional content to ensure compliance with Medical, Legal, and Regulatory (MLR) standards.
Qualifications
Advanced degree in a healthcare‑related field (MD, PharmD, PhD, or equivalent).
7+ years of experience in medical affairs or related roles within the pharmaceutical or biotech industry.
Experience supporting clinical trials and working cross‑functionally in a matrixed environment.
Strong scientific acumen, communication skills, and ability to work independently in a fast‑paced setting.
Strong understanding of regulatory and compliance frameworks (e.g., FDA, EMA).
Position Location & Compensation This is a remote role; periodic travel to conferences, team and company events is required. The anticipated salary range for this role is $270,000 – $295,000, with final compensation depending on experience, education, and geography.
As part of the I‑9 verification of authorization to work in the United States, Jade Biosciences participates in E‑Verify. To learn more about E‑Verify, please review the posted information.
Jade Biosciences is proud to be an Equal Opportunity employer. All qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected veteran status, age, or any other characteristic protected by law.
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Company Overview Jade Biosciences is focused on developing innovative, best‑in‑class therapies to address critical unmet needs in autoimmune diseases. The lead candidate, JADE101, inhibits the cytokine APRIL and is being developed for the treatment of immunoglobulin A nephropathy (IgAN). JADE101 aims to reduce harmful IgA antibodies, lower proteinuria, and preserve long‑term kidney function. A Phase 1 healthy‑volunteer study is ongoing, with interim biomarker data expected in the first half of 2026. The pipeline also includes JADE201 and an undisclosed antibody discovery program, JADE‑003, both in preclinical development.
Role Overview We are looking for a proactive and scientifically driven Director, Medical Affairs to support Jade’s clinical development programs and help establish the medical affairs function. The new position will serve as a bridge between clinical development and future commercial readiness, ensuring scientific rigor, regulatory alignment, and strategic foresight. The role reports to the Executive Medical Director, Clinical Development and is fully remote with occasional travel.
Key Responsibilities
Collaborate with internal stakeholders to develop and communicate medical plans for the therapeutic area and track progress for reporting.
Incorporate insights from scientific trends and the treatment landscape through participation in external events and activities.
Lead the development and dissemination of scientific and medical data via publications, presentations, and educational programs for healthcare professionals and other stakeholders.
Build and maintain strong relationships with KOLs, researchers, and patient advocacy groups to gather insights and inform strategy.
Manage conference calendar and coordinate onsite meetings, advisory boards, symposia, and medical education events.
Collaborate with the regulatory team to ensure all medical communications and activities comply with relevant regulations (e.g., FDA, ICH‑GCP).
Oversee or contribute to the design and implementation of studies generating real‑world evidence (RWE), health economics and outcomes research (HEOR), and other data to support product value proposition and market access efforts.
Act as a scientific consultant and collaborator across internal teams (R&D, Clinical Development, Regulatory Affairs, Commercial) to align strategies and support product development and commercialization.
Provide accurate and up‑to‑date medical information to address inquiries from healthcare professionals and external stakeholders.
Review promotional content to ensure compliance with Medical, Legal, and Regulatory (MLR) standards.
Qualifications
Advanced degree in a healthcare‑related field (MD, PharmD, PhD, or equivalent).
7+ years of experience in medical affairs or related roles within the pharmaceutical or biotech industry.
Experience supporting clinical trials and working cross‑functionally in a matrixed environment.
Strong scientific acumen, communication skills, and ability to work independently in a fast‑paced setting.
Strong understanding of regulatory and compliance frameworks (e.g., FDA, EMA).
Position Location & Compensation This is a remote role; periodic travel to conferences, team and company events is required. The anticipated salary range for this role is $270,000 – $295,000, with final compensation depending on experience, education, and geography.
As part of the I‑9 verification of authorization to work in the United States, Jade Biosciences participates in E‑Verify. To learn more about E‑Verify, please review the posted information.
Jade Biosciences is proud to be an Equal Opportunity employer. All qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected veteran status, age, or any other characteristic protected by law.
#J-18808-Ljbffr